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13518 Dst

13518

Dst

dystonin

protein-coding

Mus musculus

基因描述

Type Description
Definition dystonin

研究结论

Date Results Publications
2020-03-07 12:16:00 FLG and DST support melanoma cell growth in vitro and in vivo. Growth effects of JUP were only evident in vivo, and may be mediated, in part, by enhancing angiogenesis. In addition, growth-promoting effects of FLG and DST in vitro suggest that these genes may also support melanoma cell proliferation through angiogenesis-independent pathways. 31425296
2020-01-18 11:52:00 Our finding suggests that DST alteration may involve in the mechanism of diabetic dementia 30963337
2019-05-25 10:59:00 Microtubule instability is not central to initiation of dystonia musculorum (Dstdt) pathogenesis, though it may contribute to disease severity. Maintenance of microtubule stability in Dstdt-Tg4 dorsal root ganglia could be attributed to an upregulation in Dst-A3 expression as a compensation for the absence of Dst-A1 and -A2 in Dstdt-Tg4 sensory neurons. 29982604
2018-02-10 11:45:00 The present study identified novel mutant mice with a mild dt phenotype of sensory neurodegeneration and movement disorder. 27693510
2016-08-06 11:08:00 oligodendrocytes do not have an intrinsic requirement for neuronal dystonin for differentiation and myelination. 26886550

名称对应

Type IDs
Synonymous 2310001O04Rik, A830042E19Rik, AW554249, BP230, BPAG1-n, Bpag, Bpag1, Macf2, ah, athetoid, dt, mKIAA0728, nmf203, nmf339
Gene
UniProtKB-ID: DYST_MOUSE, S4R1P5_MOUSE
UniprotKB: Q91ZU6, S4R1P5
UniParc: UPI0000DBD9C1, UPI0004AC3F5F, UPI0002B83574, UPI0004AC3F65, UPI0000DBD9C2, UPI00005C8BBC, UPI0000D67AFE, UPI0002B83576
EMBL: AF396877, AF396878, AK037206, U22452, U25158, AC123072, AF396879, AC124386, DQ023311, AF115383, AB085694, AK051626, AC127433, DQ463750
Ensembl: ENSMUSG00000026131
KO: mmu:13518
Nucleutide sequences
EMBL-CDS: AAY46942.1, AAK83383.1, AAC52231.1, AAD22959.1, BAC34695.1, AAC52230.1, BAC29753.1, AAK83384.1, AAK83382.1, ABF00406.1, BAB93448.1
Ensembl_TRS: ENSMUST00000183302, ENSMUST00000097786, ENSMUST00000097785, ENSMUST00000183034
Protein sequencees
Ensembl_PRO: ENSMUSP00000138376, ENSMUSP00000095392, ENSMUSP00000095393, ENSMUSP00000138308
RefSeq: XP_017170205.1, XP_030102360.1, XP_017170239.1, NP_001263693.1, NP_034211.2, XP_017170140.1, XP_017170176.1, XP_006495748.1, XP_017170337.1, XP_006495749.1, XP_006495743.1, XP_017170211.1, XP_017170110.1, XP_006495747.1, NP_598594.2, XP_036014401.1, XP_006495742.1, XP_006495737.1, XP_036014447.1, XP_017170300.1, XP_006495753.1, XP_017170195.1, XP_017170178.1, XP_017170230.1, XP_017170201.1, XP_017170154.1, XP_017170165.1, XP_017170283.1, XP_017170357.1, XP_006495745.1, XP_017170124.1, NP_604443.2, XP_006495729.1, XP_006495741.1, XP_030102561.1, XP_006495754.1, XP_006495732.1, XP_006495751.1
Others
UniRef100: UniRef100_Q91ZU6, UniRef100_S4R1P5
UniRef90: UniRef90_S4R1P5, UniRef90_Q91ZU6
UniRef50: UniRef50_Q91ZU6, UniRef50_Q03001
UniGene: Mm.336625, Mm.478284, Mm.487428
CCDS: CCDS35534.1, CCDS35535.1, CCDS69875.1

全选

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